A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052116



Internal ID18794647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111671790..111716743hg38UCSC Ensembl
Innerchr9:114434070..114479023hg19UCSC Ensembl
Innerchr9:113473891..113518844hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3844954
hg1944954
hg1844954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7700n100
Supporting Variantsnssv3695051
Samples
Known GenesC9orf84
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052116
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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